SFTA2, surfactant associated 2, 389376

N. diseases: 25; N. variants: 13
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3132581
rs3132581
Entrez Id: 135656;389376;102723346
Gene Symbol: MUCL3;SFTA2;HCG21
MUCL3;SFTA2;HCG21
CUI: C1263846
Disease:
Attention deficit hyperactivity disorder 		G 0.800 GeneticVariation GWASDB Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 23453885 2013
dbSNP: rs3132581
rs3132581
Entrez Id: 135656;389376;102723346
Gene Symbol: MUCL3;SFTA2;HCG21
MUCL3;SFTA2;HCG21
CUI: C1263846
Disease:
Attention deficit hyperactivity disorder 		G 0.800 GeneticVariation GWASCAT Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 23453885 2013
dbSNP: rs115123027
rs115123027
Entrez Id: 135656;389376
Gene Symbol: MUCL3;SFTA2
MUCL3;SFTA2
CUI: C0036341
Disease:
Schizophrenia 		T 0.700 GeneticVariation GWASCAT Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect. 30285260 2019
dbSNP: rs114115252
rs114115252
Entrez Id: 389376
Gene Symbol: SFTA2
SFTA2
CUI: C0036341
Disease:
Schizophrenia 		0.700 GeneticVariation GWASCAT Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. 28540026 2017
dbSNP: rs114115252
rs114115252
Entrez Id: 389376
Gene Symbol: SFTA2
SFTA2
CUI: C0008074
Disease:
Child Development Disorders, Pervasive 		0.700 GeneticVariation GWASCAT Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. 28540026 2017
dbSNP: rs114838832
rs114838832
Entrez Id: 135656;389376
Gene Symbol: MUCL3;SFTA2
MUCL3;SFTA2
CUI: C0036341
Disease:
Schizophrenia 		A 0.700 GeneticVariation GWASCAT Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. 28540026 2017
dbSNP: rs114838832
rs114838832
Entrez Id: 135656;389376
Gene Symbol: MUCL3;SFTA2
MUCL3;SFTA2
CUI: C0008074
Disease:
Child Development Disorders, Pervasive 		A 0.700 GeneticVariation GWASCAT Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. 28540026 2017
dbSNP: rs3132580
rs3132580
Entrez Id: 135656;389376;102723346
Gene Symbol: MUCL3;SFTA2;HCG21
MUCL3;SFTA2;HCG21
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic 		A 0.700 GeneticVariation GWASDB GWAS identifies novel SLE susceptibility genes and explains the association of the HLA region. 24871463 2014
dbSNP: rs2253705
rs2253705
Entrez Id: 389376
Gene Symbol: SFTA2
SFTA2
CUI: C0019163
Disease:
Hepatitis B 		0.700 GeneticVariation GWASDB A genome-wide association study identified new variants associated with the risk of chronic hepatitis B. 23760081 2013
dbSNP: rs3132581
rs3132581
Entrez Id: 135656;389376;102723346
Gene Symbol: MUCL3;SFTA2;HCG21
MUCL3;SFTA2;HCG21
CUI: C0008074
Disease:
Child Development Disorders, Pervasive 		G 0.700 GeneticVariation GWASCAT Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 23453885 2013
dbSNP: rs3132581
rs3132581
Entrez Id: 135656;389376;102723346
Gene Symbol: MUCL3;SFTA2;HCG21
MUCL3;SFTA2;HCG21
CUI: C0005586
Disease:
Bipolar Disorder 		G 0.700 GeneticVariation GWASCAT Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 23453885 2013
dbSNP: rs3132581
rs3132581
Entrez Id: 135656;389376;102723346
Gene Symbol: MUCL3;SFTA2;HCG21
MUCL3;SFTA2;HCG21
CUI: C1269683
Disease:
Major Depressive Disorder 		G 0.700 GeneticVariation GWASCAT Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 23453885 2013
dbSNP: rs3132581
rs3132581
Entrez Id: 135656;389376;102723346
Gene Symbol: MUCL3;SFTA2;HCG21
MUCL3;SFTA2;HCG21
CUI: C0036341
Disease:
Schizophrenia 		G 0.700 GeneticVariation GWASCAT Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 23453885 2013
dbSNP: rs3132580
rs3132580
Entrez Id: 135656;389376;102723346
Gene Symbol: MUCL3;SFTA2;HCG21
MUCL3;SFTA2;HCG21
CUI: C0242379
Disease:
Malignant neoplasm of lung 		0.700 GeneticVariation GWASDB Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls. 22899653 2012
dbSNP: rs3132580
rs3132580
Entrez Id: 135656;389376;102723346
Gene Symbol: MUCL3;SFTA2;HCG21
MUCL3;SFTA2;HCG21
CUI: C0026896
Disease:
Myasthenia Gravis 		0.700 GeneticVariation GWASDB Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08. 23055271 2012
dbSNP: rs6933400
rs6933400
Entrez Id: 135656;389376
Gene Symbol: MUCL3;SFTA2
MUCL3;SFTA2
CUI: C0010068
Disease:
Coronary heart disease 		0.700 GeneticVariation GWASDB Genome-wide association study of coronary artery disease in the Japanese. 21971053 2012
dbSNP: rs3132580
rs3132580
Entrez Id: 135656;389376;102723346
Gene Symbol: MUCL3;SFTA2;HCG21
MUCL3;SFTA2;HCG21
CUI: C0017665
Disease:
Membranous glomerulonephritis 		T 0.700 GeneticVariation GWASCAT Risk HLA-DQA1 and PLA(2)R1 alleles in idiopathic membranous nephropathy. 21323541 2011
dbSNP: rs12190030
rs12190030
Entrez Id: 135656;389376;102723346
Gene Symbol: MUCL3;SFTA2;HCG21
MUCL3;SFTA2;HCG21
CUI: C1836232
Disease:
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 GeneticVariation GWASDB The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. 21051598 2010
dbSNP: rs12190030
rs12190030
Entrez Id: 135656;389376;102723346
Gene Symbol: MUCL3;SFTA2;HCG21
MUCL3;SFTA2;HCG21
CUI: C1836231
Disease:
HIV-1, RESISTANCE TO 		0.700 GeneticVariation GWASDB The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. 21051598 2010
dbSNP: rs12190030
rs12190030
Entrez Id: 135656;389376;102723346
Gene Symbol: MUCL3;SFTA2;HCG21
MUCL3;SFTA2;HCG21
CUI: C1836233
Disease:
AIDS, PROGRESSION TO 		0.700 GeneticVariation GWASDB The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. 21051598 2010
dbSNP: rs12190030
rs12190030
Entrez Id: 135656;389376;102723346
Gene Symbol: MUCL3;SFTA2;HCG21
MUCL3;SFTA2;HCG21
CUI: C1836230
Disease:
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.700 GeneticVariation GWASDB The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. 21051598 2010
dbSNP: rs3132580
rs3132580
Entrez Id: 135656;389376;102723346
Gene Symbol: MUCL3;SFTA2;HCG21
MUCL3;SFTA2;HCG21
CUI: C0042900
Disease:
Vitiligo 		0.700 GeneticVariation GWASDB Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC. 20526339 2010
dbSNP: rs12697941
rs12697941
Entrez Id: 135656;389376
Gene Symbol: MUCL3;SFTA2
MUCL3;SFTA2
CUI: C1836233
Disease:
AIDS, PROGRESSION TO 		0.700 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166 2009
dbSNP: rs12697941
rs12697941
Entrez Id: 135656;389376
Gene Symbol: MUCL3;SFTA2
MUCL3;SFTA2
CUI: C1836231
Disease:
HIV-1, RESISTANCE TO 		0.700 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166 2009
dbSNP: rs12697941
rs12697941
Entrez Id: 135656;389376
Gene Symbol: MUCL3;SFTA2
MUCL3;SFTA2
CUI: C1836230
Disease:
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.700 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166 2009